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Safety Information
11636120910
Roche
PCR ELISA, DIG-Labeling
sufficient for 50 reactions, kit of 1 (8 components), suitable for nucleic acid labeling
Synonym(s):
ELISA
Select a Size
CN¥483.72
Estimated to ship onSeptember 15, 2025Details
Select a Size
About This Item
CN¥483.72
Estimated to ship onSeptember 15, 2025Details
Recommended Products
form
solution
usage
sufficient for 50 reactions
packaging
kit of 1 (8 components)
manufacturer/tradename
Roche
technique(s)
nucleic acid labeling: suitable
shipped in
dry ice
storage temp.
−20°C
1 of 4
This Item | P9599 | P8340 | P8215 |
---|---|---|---|
form DMSO solution | form DMSO solution | form DMSO solution | form DMSO solution |
Quality Level 300 | Quality Level 300 | Quality Level 300 | Quality Level 300 |
storage temp. 2-8°C | storage temp. −20°C | storage temp. −20°C | storage temp. −20°C |
shipped in wet ice | shipped in - | shipped in - | shipped in - |
General description
Application
- In the presence of an appropriate target-specific, biotin-labeled capture probe, you can distinguish PCR products that differ by as little as a single base pair. Thus the PCR ELISA system (DIG-labeling + DIG-detection) can be used: to detect point mutations, deletions or insertions and to classify target sequences (e.g., as in HLA-typing or cell typing).
- Preparation of suitable DIG-labeled standards and addition of a colorimetric detection system will allow you to quantify PCR products.
- The microplate format used by the PCR ELISA system makes the system compatible with automated plate preparation and reading systems.
- The microplate format combined with colorimetric detection allows quantification of the amount of template present in a sample when used in combination with suitable standards.[1]
- When using appropriate capture probes, the kit can be used for the typing of a target sequence (e.g., in HLA-typing or cell typing). The microplate format makes this kit particularly suited for automation.
- The kit has been used in RT-PCR ELISA method to measure the dihydropyrimidine dehydrogenase (DPD) mRNA expression in liver and cell cycle phase distribution of bone marrow cells.[2]
Packaging
Quality
Other Notes
Kit Components Only
- PCR DIG Labeling Mix, containing 2 mM dATP, dCTP, dGTP, 1.9 mM dTTP, and 0.1 mM Digoxigenin-dUTP
- PCR Reaction Buffer, without MgCl2, 100 mM Tris/HCl, 500 mM KCl, pH 8.3 (20 °C) 10x concentrated
- MgCl2 Stock Solution 25 mM
- PCR Buffer, 100 mM Tris/HCl, 15 mM MgCl2, 500 mM KCl, pH 8.3 (20 °C) 10x concentrated
- Taq DNA Polymerase, in storage buffer: 20 mM Tris/HCl, 1 mM dithiothreitol, 0.1 mM EDTA, 0.5% Nonidet P40 (v/v), 50% Tween 20 (v/v), 0.5% glycerol (v/v), pH 8.0 (+4 °C) 5 U/μl
- Control PCR Primer Mix, specific for the human t-PA gene 125 pmol each
- Human Control DNA 1 ng/μl
- Water, PCR Grade
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 2
Flash Point(F)
does not flash
Flash Point(C)
does not flash
Regulatory Information
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Articles
Digoxigenin (DIG) labeling methods and kits for DNA and RNA DIG probes, random primed DNA labeling, nick translation labeling, 5’ and 3’ oligonucleotide end-labeling.
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